- Copying / Quantifying dropout
- per gene bias
- relationship between transcripts vs marker and observed association
- concordance of expected transcript frequency vs. observed
- QC
- min #counts /sample
- normalization
- Sets of transcripts in all cells
Unsupervised
- subclustering
- ADT, then RNA, or vice versa
- dimensionality reduction
- PCA / MDS / t-SNE / SIMILIR
- NNMF
- Autoencoder
Supervised
- random forest / ensemble methods
- others
- Interactive displa (html/browser based for audience engagement)
- traditoinal plots
- biological significance
- etc?